Pipeline: sanger-tol/sequencecomposition (1.0.0)

Launch ID: 1713881982_449fbc9a2c6b

Go through the pipeline inputs below, setting them to the values that you would like. When you're done, click Launch and your parameters will be saved.

The page shown will show a command that you can use to directly launch the workflow. For those running on a system with no internet connection, you can copy the parameters JSON to a file and use the supplied command to launch.

Nextflow command-line flags
Nextflow command-line flags

General Nextflow flags to control how the pipeline runs.

These are not specific to the pipeline and will not be saved in any parameter file. They are just used when building the `nextflow run` launch command.
Must match pattern ^[a-zA-Z0-9-_]+$

Unique name for this nextflow run

Configuration profile

Work directory for intermediate files

Resume previous run, if found

Execute the script using the cached results, useful to continue executions that was stopped by an error

Input/output options

Define where the pipeline should find input data and save output data.

Path to the Fasta file to analyze. Can be a remote location.

This file can also be compressed with Gzip.

This parameter is required

The output directory where the results will be saved. Not considered when running the pipeline with a .csv file as input.

Must match pattern ^\S+\.csv$

Path to comma-separated file containing information about the genomes to analyse. Used for bulk analysis of many genomes.

The file has to be a comma-separated file with two columns, and a header row. The columns names must be species_dir and assembly_name. An additional assembly_accession column can be provided too.